Canonical Allele Identifier: CA9725733

Gene: RSPO4

Linked Data

• dbSNP Id: rs756916549
• ExAC: 20:948618 G / A
• gnomAD v2: 20-948618-G-A
• gnomAD v4: 20-967975-G-A
• MyVariant Identifiers: chr20:g.948618G>A (hg19) ; chr20:g.967975G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967975G>A , CM000682.2:g.967975G>A	GRCh38
NC_000020.10:g.948618G>A , CM000682.1:g.948618G>A	GRCh37
NC_000020.9:g.896618G>A	NCBI36
NG_013043.1:g.39290C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.243C>T MANE Select	ENSP00000217260.4:p.Arg81=
ENST00000217260.8:c.243C>T	ENSP00000217260.4:p.Arg81=
ENST00000400634.2:c.243C>T	ENSP00000383475.2:p.Arg81=
NM_001029871.3:c.243C>T	NP_001025042.2:p.Arg81=
NM_001040007.2:c.243C>T	NP_001035096.1:p.Arg81=
XM_011529232.1:c.291C>T	XP_011527534.1:p.Arg97=
XM_011529233.1:c.291C>T	XP_011527535.1:p.Arg97=
XR_937068.1:n.363C>T
XR_937069.1:n.358C>T
XM_017027839.1:c.243C>T	XP_016883328.1:p.Arg81=
NM_001029871.4:c.243C>T MANE Select	NP_001025042.2:p.Arg81=
NM_001040007.3:c.243C>T	NP_001035096.1:p.Arg81=